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膀胱肿瘤中的p53突变与预后

p53 mutations and prognosis in bladder tumors.

作者信息

Uchida T, Wada C, Ishida H, Wang C, Egawa S, Yokoyama E, Kameya T, Koshiba K

机构信息

Department of Urology, Kitasato University School of Medicine, Kanagawa, Japan.

出版信息

J Urol. 1995 Apr;153(4):1097-104.

PMID:7869472
Abstract

The incidence of loss of heterozygosity on chromosome 17p and p53 gene mutations was assessed in 43 bladder tumor patients. Histological findings, cigarette smoking and prognosis were examined for possible correlation with the presence or absence of loss of heterozygosity on 17p and p53 mutations. Of 20 informative cases 10 (50.0%) showed loss of heterozygosity of 17p13, including 9 (90.0%) with disease beyond stage pT2. The p53 mutations were detected in 20 of 43 patients (46.5%), including 9 (95.0%) with disease beyond grade 2 and 17 (85.0%) with cancer beyond stage pT2. The incidence of p53 gene mutations was not significantly influenced by habitual smoking but G:C to T:A substitutions, often observed in lung cancers, were detected only in mutations from smokers (5 of 10 or 50%, p < 0.05). Groups with and without loss of heterozygosity showed essentially the same results, while significant differences were found for groups with grades 1 and 2 to 3 (p < 0.05) cancer, stages pT1 and pT2 to 4 (p < 0.01) disease, and with and without p53 gene mutations (p < 0.01, Cox-Mantel test). Genetic alternation in chromosome 17p and p53 mutations would, thus, appear to occur more frequently in high grade and invasive bladder tumors. Cigarette smoking may possibly be a determining factor of mutations of the p53 gene in bladder tumors. Our results indicate that an unfavorable prognostic factor may possibly be linked not only to histopathological findings but the presence of a p53 mutation in bladder tumors as well. Accordingly, mutations of the p53 gene may be deeply involved in late events of tumorigenesis and possibly useful as ideal molecular markers for prognosis in bladder tumors.

摘要

对43例膀胱肿瘤患者评估了17号染色体短臂杂合性缺失(LOH)及p53基因突变的发生率。研究了组织学结果、吸烟情况及预后与17号染色体短臂杂合性缺失及p53突变的有无之间的可能相关性。在20例信息充分的病例中,10例(50.0%)显示17p13杂合性缺失,其中9例(90.0%)疾病分期超过pT2期。43例患者中有20例(46.5%)检测到p53突变,其中9例(95.0%)肿瘤分级超过2级,17例(85.0%)癌症分期超过pT2期。p53基因突变的发生率不受习惯性吸烟的显著影响,但在肺癌中常见的G:C到T:A替换仅在吸烟者的突变中检测到(10例中有5例,即50%,p<0.05)。有和没有杂合性缺失的组结果基本相同,而在肿瘤分级为1级和2至3级(p<0.05)、分期为pT1和pT2至4期(p<0.01)以及有和没有p53基因突变的组(p<0.01,Cox-Mantel检验)中发现了显著差异。因此,17号染色体短臂的基因改变及p53突变似乎在高级别和浸润性膀胱肿瘤中更频繁发生。吸烟可能是膀胱肿瘤中p53基因突变的一个决定性因素。我们的结果表明,不良预后因素可能不仅与组织病理学结果有关,还与膀胱肿瘤中p53突变的存在有关。因此,p53基因突变可能深度参与肿瘤发生的晚期事件,并可能作为膀胱肿瘤预后的理想分子标志物。

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